ENST00000644719.2:c.936T>A
MANE Select
|
ENSP00000496625.1:p.Pro312=
|
|
ENST00000418967.6:c.936T>A
|
ENSP00000408860.2:p.Pro312=
|
|
ENST00000435122.3:c.846T>A
|
ENSP00000415043.2:p.Pro282=
|
|
ENST00000479074.5:n.994T>A
|
|
|
ENST00000479730.5:n.1052T>A
|
|
|
ENST00000483041.5:n.1105T>A
|
|
|
ENST00000486063.5:n.919-204T>A
|
|
|
NM_000500.7:c.936T>A
|
NP_000491.4:p.Pro312=
|
|
NM_001128590.3:c.846T>A
|
NP_001122062.3:p.Pro282=
|
|
XM_011514314.1:c.531T>A
|
XP_011512616.1:p.Pro177=
|
|
NM_000500.9:c.936T>A
MANE Select
|
NP_000491.4:p.Pro312=
|
|
NM_001368143.1:c.531T>A
|
NP_001355072.1:p.Pro177=
|
|
NM_001368144.1:c.531T>A
|
NP_001355073.1:p.Pro177=
|
|
NM_001128590.4:c.846T>A
|
NP_001122062.3:p.Pro282=
|
|
NM_001368143.2:c.531T>A
|
NP_001355072.1:p.Pro177=
|
|
NM_001368144.2:c.531T>A
|
NP_001355073.1:p.Pro177=
|
|